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Acetamide, N-2-benzothiazolyl-2-hydrazino- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

365544-22-5

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365544-22-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 365544-22-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,5,5,4 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 365544-22:
(8*3)+(7*6)+(6*5)+(5*5)+(4*4)+(3*4)+(2*2)+(1*2)=155
155 % 10 = 5
So 365544-22-5 is a valid CAS Registry Number.

365544-22-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-((hydrazinoacetyl)amino)benzothiazole

1.2 Other means of identification

Product number -
Other names ACETAMIDE,N-2-BENZOTHIAZOLYL-2-HYDRAZINYL-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:365544-22-5 SDS

365544-22-5Relevant academic research and scientific papers

Synthesis and biological evaluation of 2-aminobenzothiazole derivatives

Srivastava,Sen

experimental part, p. 1583 - 1586 (2009/04/10)

As a part of systematic investigation of synthesis and biologically active compounds of 2-amino benzothiazoles, several new [(2″-substituted aryl)-4″-oxo-1″,3″-thiazolidine-3″-iminoacetyl] -2-aminobenzothiazole 5 and [(5″-arylidene-2″-substituted aryl-4″-oxo-1″,3″-thiazolidine)-3″-iminoacetyl] -2-aminobenzothiazole 6 from 2-aminobenzothiazole have been synthesized. All the synthesized products are evaluated for their antibacterial activity against Bacillus substilis, Escherichia coli, Klebsiella pneumoniae and Staphylococcus aureus and antifungal activity against Aspergillus niger, Aspergillus flavus, Fusarium oxisporum and Trichoderma viride. The structures of all the synthesized compounds have been determined by spectral and chemical methods.

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